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第 1 期                 陆秀红 等:番茄响应南方根结线虫侵染相关转录因子的初步分析                                        69

                    sis of bHLH transcription factor and involvement in the infec⁃  cum)[J/OL].BMC genomics,2015,16(1):39[2022-12-08].
                    tion  by  yellow  leaf  curl  virus  in  tomato (Solanum  lycopersi‑  https://doi.org/10.1186/s12864-015-1249-2.


                     Preliminary analysis of transcription factors associated with tomato

                                   response to infection of Meloidogyne incognita



                                                       1
                                        1
                                                                   1
                                                                                  2
                             LU Xiuhong ,HUANG Jinling ,QIN Liping ,LIU Zhengrong ,LIU Zhiming  1
                              1.Institute of Plant Protection, Guangxi Academy of Agricultural Sciences/
                          Key Laboratory of Green Prevention and Control on Fruits and Vegetables in South
                       China Ministry of Agriculture and Rural Affairs/Guangxi Key Laboratory of Biology for
                                      Crop Diseases and Insect Pests,Nanning 530007, China;
                               2.College of Agricultural, Guangxi University, Nanning 530005, China



                   Abstract  In order to explore the gene expression pattern at transcriptional level of tomato after inocu⁃
               lated with Meloidogyne incognita, transcriptome sequencing was performed on tomato root at  6 h, 12 h,
               24 h and 48 h after inoculated with 2nd instar larvae of root-knot nematode. The key transcription factor re⁃
               lated to the tomato response to the infection of M. incognita were analyzed and the sequencing results were
               verified by quantitative real-time PCR. The results showed that 350, 390, 580, 1 154 genes were differen⁃
               tially expressed at 6 h, 12 h, 24 h and 48 h after inoculation, and 11, 11, 19 and 50 transcription factors
               were  differentially  expressed,  respectively.  They  belonged  to  15  transcription  factor  families,  of  which
               MYB  family  and  bHLH  family  are  the  most  abundant  with  20  genes,  followed  by  ERF  family  with  19
               genes, WRKY family with 15 genes, and bZIP family with 9 genes. Further studies showed that the tran⁃
               scription  factors  of  ERF,WRKY,MYB  and  bHLH  family  were  the  most  differentially  expressed.
               Solyc03g005520,  Solyc02g094270  and  Solyc09g066350  were  significantly  up  regulated  and  the  log 2FC  at
               48  h  after  inoculation  was  9.16,  6.49  and  6.33,  respectively.  Solyc03g005520,  Solyc02g094270  and
               Solyc09g066350 were significantly down regulated, and log 2FC at 48 h after inoculation was -2.60,-1.72
               and -1.70,respectively. The results of qRT-PCR analysis showed that the expression trend of six random⁃
               ly selected genes was consistent with the sequencing results. The results of this study suggest that the tran⁃
               scription factors of ERF, WRKY and bHLH family may be involved in the interaction between tomato and
               M. incognita, and play an important regulatory role in tomato response to the infection of M. incognita.
                   Keywords  tomato; transcription factor; Meloidogyne incognita; nematode infection; qRT-PCR


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